用于蛋白质-药物相互作用分析的新兴亲和方法。

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
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引用次数: 0

摘要

蛋白质与药物相互作用的研究在了解药物机制、确定新的药物靶点和生物标志物、促进药物开发和疾病治疗方面发挥着至关重要的作用。近年来,随着质谱、核磁共振、拉曼光谱等技术的快速发展和深入应用,各种蛋白质-药物相互作用研究方法取得了重大进展。这些进步提高了分析方法的灵敏度、精确度、准确性和适用性,使药物-蛋白质相互作用网络的建立成为可能。这篇综述讨论了各种新兴的研究方法,如原生质谱法、红外光谱法、核磁共振和光谱法,采用表面增强拉曼、电化学和磁阻信号的生物传感器技术,以及亲和磁悬浮和亲和色谱法。文章还深入探讨了这些技术的原理、应用、优势和局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging affinity methods for protein-drug interaction analysis

The study of protein-drug interaction plays a crucial role in understanding drug mechanisms, identifying new drug targets and biomarkers, and facilitating drug development and disease treatment. In recent years, significant progress has been made in various protein-drug interaction research methods due to the rapid development and in-depth application of mass spectrometry, nuclear magnetic resonance, Raman spectroscopy, and other technologies. The progress has enhanced the sensitivity, precision, accuracy, and applicability of analytical methods, enabling the establishment of drug-protein interaction networks. This review discusses various emerging research methods, such as native mass spectrometry, infrared spectroscopy, nuclear magnetic resonance and spectrum, biosensor technologies employing surface enhanced Raman, electrochemistry, and magneto resistive signals, as well as affinity magnetic levitation and affinity chromatography. The article also delves into the principles, applications, advantages, and limitations of these technologies.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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